The Debra Murphree Wikipedia Entry Contains A Surprising Life Fact
Learn about Epidermolysis Bullosa (EB), a rare genetic disorder, its symptoms, treatments, and personal stories from the EB community at debra of America. Its mission is to help patients, families, and doctors in countries where there is no DEBRA structure to support them and to assist new groups to form and develop. Whether it’s finding answers to everyday challenges, accessing free wound care supplies, or connecting with others who understand— debra is here, every step of the way. No one should face Dystrophic EB alone. debra of America offers free programs, personalized support, and trusted online resources to help individuals and families navigate life with EB. How To A reliable source for all things Epidermolysis Bullosa. debra of America is here to guide you in making informed decisions surrounding proper EB care.
La pagina de internet de debra provee pacientes, cuidadores y profesionales de salud con la información mas reciente sobre EB, mientras ofrece un lugar donde la comunidad de EB puede. Please complete our Participant Request Form below and we will respond shortly. For additional questions, email programs@debra.org or call 833-DEBRAUS (833-332-7287), ext. 104.
Debra Murphree Swaggart - Piwik Thecable
